Also known as: Soft tissue tumors, Askin tumor, peripheral primitive neuroectodermal tumor
What is Ewing sarcoma?
Ewing sarcoma is a rare type of cancer that usually develops in the bones or soft tissue around the bones (cartilage/nerves) of children 10-20 years of age. The pelvis, femur, ribs, or shoulders are often where they start.
What causes Ewing sarcoma?
The cause of Ewing sarcoma is not entirely clear. It doesn't appear to run in families but probably occurs following a gene mutation from exposure to harmful environmental factors (chemicals, radiation etc.).
What are the signs and symptoms of Ewing sarcoma?
Pain, fever and swelling for a long time where the tumor presents; bone breaks without a reason, difficulty with bladder control, and tiredness and weight loss may be presenting features.
What are Ewing sarcoma care options?
Treatment for Ewing sarcoma may include surgery, radiation therapy, chemotherapy, targeted therapy or some combination of these treatments.
This page was last updated on: 5/23/2018 11:13:28 AM
The Nicklaus Children’s Cancer & Blood Disorders Center, together with the Brain Institute is proud to host this free event designed to deliver education, support and guidance for children diagnosed with brain tumors and their caregivers. Learn more.
In this edition of Talkin' Kids Health we will discuss cancer effects and the survivorship program at Nicklaus Children's with Dr. Haneen Abdella, Pediaric Oncolgoist at Nicklaus Children's and Kristen Mendez, ARNP and Manager of the Survivorship Program. Learn more.
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